Variant ID: 12-102590473-C-A

NM_002674.2(PMCH):c.455G>T;(p.Arg152Ile)

This variant was identified in 1 publication




Publications:


A Review of Single-Nucleotide Polymorphisms in Orexigenic Neuropeptides Targeting G Protein-Coupled Receptors.

Acs Chemical Neuroscience
MD Ericson, C Haskell-Luevano
Publication Date: 2018-06-20

Variant appearance in text: rs781675279
PubMed Link: 29714060
Variant Present in the following documents:
  • Main text
View BVdb publication page



Alternative transcript annotations:

Transcript cDNA Protein Consequence Exon Intron
ENST00000327680.2 c.*404C>A - 3_prime_UTR_variant 12/12 -
ENST00000329406.4 c.455G>T p.Arg152Ile missense_variant 3/3 -
ENST00000378128.3 c.*672C>A - 3_prime_UTR_variant 7/7 -
ENST00000412715.2 c.*672C>A - 3_prime_UTR_variant 6/6 -
ENST00000417507.2 c.*736C>A - 3_prime_UTR_variant 7/7 -
ENST00000457614.2 c.*1458C>A - 3_prime_UTR_variant,NMD_transcript_variant 8/8 -
ENST00000535811.1 n.799C>A - non_coding_transcript_exon_variant 2/2 -
NM_001319988.1 c.*404C>A - 3_prime_UTR_variant 12/12 -
NM_001319993.1 c.*404C>A - 3_prime_UTR_variant 12/12 -
NM_001319994.1 c.*404C>A - 3_prime_UTR_variant 11/11 -
NM_002674.4 c.455G>T p.Arg152Ile missense_variant 3/3 -
NM_017915.4 c.*404C>A - 3_prime_UTR_variant 11/11 -
NR_135123.1 n.1343C>A - non_coding_transcript_exon_variant 5/5 -